Cas 147555-70-2,(Z)-7-[(1S,2R,3S,5R)-2-(tert-Butyl-diphenyl-silanyloxymethyl)-3,5-dihydroxy-cyclopentyl]-hept-5-enoic acid methyl ester

147555-70-2

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Basic information

Product Name: (Z)-7-[(1S,2R,3S,5R)-2-(tert-Butyl-diphenyl-silanyloxymethyl)-3,5-dihydroxy-cyclopentyl]-hept-5-enoic acid methyl ester
Synonyms: (Z)-7-[(1S,2R,3S,5R)-2-(tert-Butyl-diphenyl-silanyloxymethyl)-3,5-dihydroxy-cyclopentyl]-hept-5-enoic acid methyl ester
CAS NO:147555-70-2
Molecular Formula:
Molecular Weight: 510.746
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (Z)-7-[(1S,2R,3S,5R)-2-(tert-Butyl-diphenyl-silanyloxymethyl)-3,5-dihydroxy-cyclopentyl]-hept-5-enoic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (Z)-7-[(1S,2R,3S,5R)-2-(tert-Butyl-diphenyl-silanyloxymethyl)-3,5-dihydroxy-cyclopentyl]-hept-5-enoic acid methyl ester(147555-70-2)
EPA Substance Registry System: (Z)-7-[(1S,2R,3S,5R)-2-(tert-Butyl-diphenyl-silanyloxymethyl)-3,5-dihydroxy-cyclopentyl]-hept-5-enoic acid methyl ester(147555-70-2)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 147555-70-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 147555-70-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,5,5 and 5 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 147555-70:
(8*1)+(7*4)+(6*7)+(5*5)+(4*5)+(3*5)+(2*7)+(1*0)=152
152 % 10 = 2
So 147555-70-2 is a valid CAS Registry Number.

147555-70-2Upstream product

147555-70-2Downstream Products

147555-67-7 (Z)-7-[(1S,5R,6S,7R)-7-(tert-Butyl-diphenyl-silanyloxymethyl)-3-oxo-2,4-dioxa-bicyclo[3.2.1]oct-6-yl]-hept-5-enoic acid methyl ester

147555-70-2Relevant academic research and scientific papers

Synthesis of (±)-15-deoxy-Δ12,14-prostaglandin J2 and Δ12-prostaglandin J2 15-acetate methyl esters

Vostrikov, N. S.,Lobko, I. F.,Miftakhov, M. S.,Ishimova, D. U.

, p. 1 - 9 (2015)

A new synthetic approach to 15-deoxy-Δ12,14-prostaglandin J2 and related compounds starting from Corey (±)-lactone diol has been developed. The key stage of this approach includes synthesis of a prostaglandin derivative possessing le

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